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Atomfair 2,6-Dimethyl-3-nitropyridine C7H8N2O2
Description 2,6-Dimethyl-3-nitropyridine (CAS No. 15513-52-7) is a high-purity nitropyridine derivative with the molecular formula C7H8N2O2. This compound is a valuable intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. Its structure features a nitro group at the 3-position and methyl groups at the 2- and 6-positions of the pyridine ring, offering unique reactivity for nucleophilic substitution and reduction reactions. Available in >98% purity (HPLC), it is supplied as a crystalline solid with strict quality control to ensure consistency for sensitive applications. Suitable for use in cross-coupling reactions, heterocyclic chemistry, and as a precursor for bioactive molecules. Store in a…
Description
Description
2,6-Dimethyl-3-nitropyridine (CAS No. 15513-52-7) is a high-purity nitropyridine derivative with the molecular formula C7H8N2O2. This compound is a valuable intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. Its structure features a nitro group at the 3-position and methyl groups at the 2- and 6-positions of the pyridine ring, offering unique reactivity for nucleophilic substitution and reduction reactions. Available in >98% purity (HPLC), it is supplied as a crystalline solid with strict quality control to ensure consistency for sensitive applications. Suitable for use in cross-coupling reactions, heterocyclic chemistry, and as a precursor for bioactive molecules. Store in a cool, dry place under inert conditions.
- CAS No: 15513-52-7
- Molecular Formula: C7H8N2O2
- Molecular Weight: 152.15
- Exact Mass: 152.058577502
- Monoisotopic Mass: 152.058577502
- IUPAC Name: 2,6-dimethyl-3-nitropyridine
- SMILES: CC1=NC(=C(C=C1)[N+](=O)[O-])C
- Synonyms: 2,6-Dimethyl-3-nitropyridine, 15513-52-7, EINECS 239-543-5, DTXSID10165816, NSC 88939
Application
2,6-Dimethyl-3-nitropyridine serves as a versatile building block in medicinal chemistry for the synthesis of nitrogen-containing heterocycles. It is employed in the development of pharmaceutical candidates, particularly for kinase inhibitors and antimicrobial agents. The nitro group facilitates further functionalization via reduction to amines or participation in cyclization reactions. Researchers also utilize it in material science for designing pyridine-based ligands and coordination complexes.
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